🛠 Tech Stack

💼 About This Role

You'll work directly with a single sponsor as a Biostatistics consultant for complex clinical trials, while enjoying the security and career opportunities of a global CRO. You will independently design protocols, develop statistical analysis plans, and perform analyses for regulatory submissions. This role offers the flexibility of fully remote work within the UK.

🎯 What You'll Do

• Design early/late-stage clinical protocols across multiple therapeutic areas
• Develop and write statistical analysis plans
• Perform statistical analyses for interim and final regulatory reports
• Support submission activities including integrated safety and efficacy summaries

📋 Requirements

• MS or PhD in Statistics or Biostatistics
• PhD + 6 years or MS + 11 years clinical trial experience in biotech/pharma
• Hands-on Phase I/II/III clinical trial experience
• Proficient in SAS programming

✨ Nice to Have

• Excellence in R programming
• Experience with regulatory submissions in US, Europe, Japan, or Rest of World

🎁 Benefits & Perks

• 🏖️ Remote work within UK
• 💼 Contract stability with a global CRO
• 📈 Career development through continuous training

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Submit CV· 1 day
2. 2Phone interview· 30 min
3. 3Client interview· 1 hour